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作 者:卢春丽[1] 伏再辉[1] 刘凤兰[1] 秦金伟[1] 何乡陵[1] 尹笃林[1]
机构地区:[1]湖南师范大学化学化工学院精细催化合成研究所,中国长沙410081
出 处:《湖南师范大学自然科学学报》2010年第2期72-76,共5页Journal of Natural Science of Hunan Normal University
基 金:国家自然科学基金资助项目(20873040;20573035)
摘 要:设计合成了一系列四齿8-羟基喹啉铜配合物(Q2CuⅡ),发现这些铜配合物能有效催化双氧水选择氧化甲苯反应,主要获得芳环上的羟基化产物邻和对甲酚(选择性约80%).Q2CuⅡ配合物的取代基对催化活性有明显影响,其中2,8-二羟基喹啉铜显示最好的活性,通过优化反应条件如反应温度、催化剂、氧化剂用量以及乙腈和水的体积比,获得了20.6%的甲苯转化率和80%甲酚选择性.基于液体紫外对反应的监控结果,推测了Q2CuⅡ催化双氧水氧化甲苯的机理.A series of 8-quinolinolato copper(Ⅱ) complexes(Q2CuⅡ) have been synthesized and characterized by IR and UV-Vis spectrocopy.These Q2CuⅡ catalysts were found to be active and selective for the oxidation of toluene with aqueous hydrogen peroxide(H2O2) in the presence of acetonitrile/water(1∶1) at 70 ℃,mainly affording a highly hydroxylated products o-and p-cresols with an approximate selectivity of 80%.Among the Q2CuⅡ catalysts examined,the 2,8-dihydroxyl-Q2CuⅡ showed the best activity with the toluene conversion of 20.6 %.The effect of amount of catalyst,reaction temperature and ratio of acetonitrile/water on this oxidation process were also investigated.Based on the UV-Vis characterization,a possible mechanism for the Q2CuⅡ catalytic system was also proposed.
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